Antisense Peptide Nucleic Acid-Diaminobutanoic Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity against Gram-Negative Bacteria

Precision antisense antibacterial agents may be developed into novel antibiotics in the fight against multidrugresistant Gram-negative bacteria. In this study, a series of diaminobutanoic acid (DAB) dendrons are presented as novel carriers for the delivery of antisense antibacterial peptide nucleic acids (PNAs). The dendron-PNA conjugates targeting the essential acpP gene exhibit specific antisense antimicrobial bactericidal activity against Escherichia coli and Klebsiella pneumoniae at one-digit micromolar concentrations, while showing low toxicity to human cells. One compound selected from a structure-activity relationship series showed high stability in mouse and human serum (t1/2 ??? 24 h) as well as in vivo activity against a multidrug-resistant, extended spectrum beta-lactamase-producing E. coli in a murine peritonitis model. The compound was also well tolerated in mice upon i.v. administration up to a dose of 20 mg/kg, and in vivo fluorescence imaging indicated clearance via renal excretion with slight accumulation in the kidneys and liver. Thus, DAB-based dendrons constitute a promising new chemistry platform for development of effective delivery agents for antibacterial drugs with possible in vivo use.

Automated summary

This study presents a series of diaminobutanoic acid (DAB) dendrons as novel carriers for the delivery of antisense antibacterial peptide nucleic acids (PNAs). These dendron-PNA conjugates exhibit specific antisense antimicrobial bactericidal activity against Escherichia coli and Klebsiella pneumoniae, while showing low toxicity to human cells. One selected compound shows high stability in mouse and human serum, and demonstrates in vivo activity against a multidrug-resistant E. coli.